Thaipetaline

Details

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Internal ID f5e7757b-77c0-45ef-80de-b4c047b98a23
Taxonomy Alkaloids and derivatives > Protoberberine alkaloids and derivatives
IUPAC Name (13aS)-2,3,9-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-4,10-diol
SMILES (Canonical) COC1=C(C(=C2CCN3CC4=C(CC3C2=C1)C=CC(=C4OC)O)O)OC
SMILES (Isomeric) COC1=C(C(=C2CCN3CC4=C(C[C@H]3C2=C1)C=CC(=C4OC)O)O)OC
InChI InChI=1S/C20H23NO5/c1-24-17-9-13-12(18(23)20(17)26-3)6-7-21-10-14-11(8-15(13)21)4-5-16(22)19(14)25-2/h4-5,9,15,22-23H,6-8,10H2,1-3H3/t15-/m0/s1
InChI Key MAGPJVVGBCSWPF-HNNXBMFYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H23NO5
Molecular Weight 357.40 g/mol
Exact Mass 357.15762283 g/mol
Topological Polar Surface Area (TPSA) 71.40 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Thaipetaline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7673 76.73%
Caco-2 + 0.8179 81.79%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.7387 73.87%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.9233 92.33%
OATP1B3 inhibitior + 0.9287 92.87%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.5954 59.54%
P-glycoprotein inhibitior - 0.7374 73.74%
P-glycoprotein substrate - 0.5874 58.74%
CYP3A4 substrate + 0.5986 59.86%
CYP2C9 substrate + 0.7825 78.25%
CYP2D6 substrate + 0.8432 84.32%
CYP3A4 inhibition - 0.8818 88.18%
CYP2C9 inhibition - 0.9112 91.12%
CYP2C19 inhibition - 0.5647 56.47%
CYP2D6 inhibition + 0.6315 63.15%
CYP1A2 inhibition + 0.7216 72.16%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.9334 93.34%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6344 63.44%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9356 93.56%
Skin irritation - 0.7640 76.40%
Skin corrosion - 0.9407 94.07%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3898 38.98%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8888 88.88%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.8668 86.68%
Acute Oral Toxicity (c) II 0.4895 48.95%
Estrogen receptor binding + 0.6297 62.97%
Androgen receptor binding + 0.5542 55.42%
Thyroid receptor binding + 0.7024 70.24%
Glucocorticoid receptor binding + 0.7055 70.55%
Aromatase binding - 0.7086 70.86%
PPAR gamma - 0.5129 51.29%
Honey bee toxicity - 0.8825 88.25%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.3996 39.96%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.30% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.28% 96.09%
CHEMBL217 P14416 Dopamine D2 receptor 97.62% 95.62%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 96.56% 93.40%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 92.22% 91.79%
CHEMBL5747 Q92793 CREB-binding protein 91.53% 95.12%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.19% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.56% 94.45%
CHEMBL2056 P21728 Dopamine D1 receptor 89.50% 91.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.49% 95.56%
CHEMBL3438 Q05513 Protein kinase C zeta 89.43% 88.48%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.87% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.51% 95.89%
CHEMBL2535 P11166 Glucose transporter 87.65% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.28% 93.99%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 86.61% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.30% 89.62%
CHEMBL4208 P20618 Proteasome component C5 85.95% 90.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.74% 91.03%
CHEMBL2581 P07339 Cathepsin D 84.96% 98.95%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.69% 82.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.22% 99.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.15% 92.94%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.00% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.15% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.17% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Annona squamosa
Fissistigma balansae
Polyalthia stenopetala

Cross-Links

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PubChem 15377962
NPASS NPC312025
LOTUS LTS0210700
wikiData Q105160321